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Prolonged versus standard native E. coli asparaginase therapy in childhood acute lymphoblastic leukemia and non-Hodgkin lymphoma: final results of the EORTC-CLG randomized phase III trial 58951.
Mondelaers, Veerle; Suciu, Stefan; De Moerloose, Barbara; Ferster, Alina; Mazingue, Françoise; Plat, Geneviève; Yakouben, Karima; Uyttebroeck, Anne; Lutz, Patrick; Costa, Vitor; Sirvent, Nicolas; Plouvier, Emmanuel; Munzer, Martine; Poirée, Maryline; Minckes, Odile; Millot, Frédéric; Plantaz, Dominique; Maes, Philip; Hoyoux, Claire; Cavé, Hélène; Rohrlich, Pierre; Bertrand, Yves; Benoit, Yves.
Afiliación
  • Mondelaers V; Department of Pediatric Hematology-Oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent University, Belgium veerle.mondelaers@uzgent.be.
  • Suciu S; EORTC Headquarters, Brussels, Belgium.
  • De Moerloose B; Department of Pediatric Hematology-Oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent University, Belgium.
  • Ferster A; Department of Pediatric Hematology-Oncology, Children's University Hospital Queen Fabiola, Université Libre de Bruxelles (ULB), Belgium.
  • Mazingue F; Department of Pediatric Hematology-Oncology, CHRU, Lille, France.
  • Plat G; Department of Pediatric Hematology-Oncology, CHU-Hopital Purpan, Toulouse, France.
  • Yakouben K; Department of Pediatric Hematology, Robert Debré Hospital, AP-HP, Paris, France.
  • Uyttebroeck A; Department of Pediatric Hematology-Oncology, University Hospital Gasthuisberg, Leuven, Belgium.
  • Lutz P; Department of Pediatric Hematology-Oncology, University Hospital Hautepierre, Strasbourg, France.
  • Costa V; Department of Pediatrics, Portuguese Oncology Institute, Porto, Portugal.
  • Sirvent N; Department of Pediatric Hematology-Oncology, CHU, Montpellier, France.
  • Plouvier E; Pediatric Hematology Unit, CHU Jean Minjoz Hospital, Besançon, France.
  • Munzer M; Department of Pediatric Hematology-Oncology, American Memorial Hospital, Reims, France.
  • Poirée M; Department of Pediatric Hematology-Oncology, CHU Lenval, Nice, France.
  • Minckes O; Department of Pediatric Hematology-Oncology, CHU, Caen, France.
  • Millot F; Pediatric Oncology Unit, University Hospital, Poitiers, France.
  • Plantaz D; Department of Pediatric Oncology, University Hospital, Grenoble, France.
  • Maes P; Department of Pediatrics, University Hospital Antwerp, Belgium.
  • Hoyoux C; Department of Pediatrics, CHR de la Citadelle, Liège, Belgium.
  • Cavé H; Department of Genetics, Assistance Publique des Hôpitaux de Paris (AP-HP), Robert Debré Hospital, Paris, France.
  • Rohrlich P; INSERM UMR 1131, University Institute of Hematology, University Paris Diderot, Paris Sorbonne Cité, France.
  • Bertrand Y; Department of Pediatric Hematology-Oncology, CHU Lenval, Nice, France.
  • Benoit Y; Institute of Pediatric Hematology and Oncology (IHOP), Hospices Civils de Lyon, and University Lyon 1, France.
Haematologica ; 102(10): 1727-1738, 2017 10.
Article en En | MEDLINE | ID: mdl-28751566
ABSTRACT
Asparaginase is an essential component of combination chemotherapy for childhood acute lymphoblastic leukemia and non-Hodgkin lymphoma. The value of asparaginase was further addressed in a group of non-very high-risk patients by comparing prolonged (long-asparaginase) versus standard (short-asparaginase) native E. coli asparaginase treatment in a randomized part of the phase III 58951 trial of the European Organization for Research and Treatment of Cancer Children's Leukemia Group. The main endpoint was disease-free survival. Overall, 1,552 patients were randomly assigned to long-asparaginase (775 patients) or short-asparaginase (777 patients). Patients with grade ≥2 allergy to native E. coli asparaginase were switched to equivalent doses of Erwinia or pegylated E. coli asparaginase. The 8-year disease-free survival rate (±standard error) was 87.0±1.3% in the long-asparaginase group and 84.4±1.4% in the short-asparaginase group (hazard ratio 0.87; P=0.33) and the 8-year overall survival rate was 92.6±1.0% and 91.3±1.2% respectively (hazard ratio 0.89; P=0.53). An exploratory analysis suggested that the impact of long-asparaginase was beneficial in the National Cancer Institute standard-risk group with regards to disease-free survival (hazard ratio 0.70; P=0.057), but far less so with regards to overall survival (hazard ratio 0.89). The incidences of grade 3-4 infection during consolidation (25.2% versus 14.4%) and late intensification (22.6% versus 15.9%) and the incidence of grade 2-4 allergy were higher in the long-asparaginase arm (30% versus 21%). Prolonged native E. coli asparaginase therapy in consolidation and late intensification for our non-very high-risk patients did not improve overall outcome but led to an increase in infections and allergy. This trial was registered at www.clinicaltrials.gov as #NCT00003728.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Asparaginasa / Linfoma no Hodgkin / Leucemia-Linfoma Linfoblástico de Células Precursoras Tipo de estudio: Clinical_trials / Diagnostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Haematologica Año: 2017 Tipo del documento: Article País de afiliación: Bélgica

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Asparaginasa / Linfoma no Hodgkin / Leucemia-Linfoma Linfoblástico de Células Precursoras Tipo de estudio: Clinical_trials / Diagnostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Haematologica Año: 2017 Tipo del documento: Article País de afiliación: Bélgica